Canonical Allele Identifier: CA2660314965

Gene: CNGA3

Linked Data

• gnomAD v4: 2-98389787-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98389787G>A , CM000664.2:g.98389787G>A	GRCh38
NC_000002.11:g.99006250G>A , CM000664.1:g.99006250G>A	GRCh37
NC_000002.10:g.98372682G>A	NCBI36
NG_009097.1:g.48633G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.566+13G>A MANE Select	ENSP00000272602.2:n.566+13G>A
ENST00000272602.6:c.566+13G>A	ENSP00000272602.2:n.566+13G>A
ENST00000393504.5:c.566+13G>A	ENSP00000377140.1:n.566+13G>A
ENST00000409937.1:c.578+13G>A	ENSP00000386761.1:n.578+13G>A
ENST00000436404.6:c.512+13G>A	ENSP00000410070.2:n.512+13G>A
NM_001079878.1:c.512+13G>A	NP_001073347.1:n.512+13G>A
NM_001298.2:c.566+13G>A	NP_001289.1:n.566+13G>A
XM_006712243.2:c.677+13G>A	XP_006712306.1:n.677+13G>A
XM_011510554.1:c.731+13G>A	XP_011508856.1:n.731+13G>A
XM_011510554.2:c.731+13G>A	XP_011508856.1:n.731+13G>A
NM_001079878.2:c.512+13G>A	NP_001073347.1:n.512+13G>A
NM_001298.3:c.566+13G>A MANE Select	NP_001289.1:n.566+13G>A